BUPROPION HYDROCHLORIDE (BUPROPION HYDROCHLORIDE) — FDA Approval ANDA200695 (SUN PHARM)
BUPROPION HYDROCHLORIDE (BUPROPION HYDROCHLORIDE) — FDA Approval ANDA200695 (SUN PHARM) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: BUPROPION HYDROCHLORIDE; Active ingredients: BUPROPION HYDROCHLORIDE; Application number: ANDA200695.
| Brand name | BUPROPION HYDROCHLORIDE |
|---|---|
| Active ingredients | BUPROPION HYDROCHLORIDE |
| Application number | ANDA200695 |
| Sponsor | SUN PHARM |
| Dosage form | TABLET, EXTENDED RELEASE |
| Route | ORAL |
| Marketing status | Discontinued |
| Products in application | 1 |
| First approval date | 20141218 |
| Source | openFDA Drugs@FDA |
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